Most of you may know someone with the debilitating disease, Multiple Sclerosis, or at least heard of the disease. MS is notorious for creating extreme fatigue, weakness, numbness or tingling that eventually leads to a person becoming dependent on a cane, walker, wheelchair or even worse, bed ridden. It has stripped so many people of their freedom of independence, hopes and dreams.
What many of you may not know is that my mother, Elaine DeLack, has Multiple Sclerosis. She was diagnosed in 1988 and at one point even encouraged to use a walker as she was continuously falling due to extreme fatigue. You read that correct.... Elaine DeLack, a woman who today rides horses, does at least 30 minutes of hard cardio a day, and runs up and down the hills in her pasture leading my two year old daughter on her pony, has had MS for 22 years.
Why is it that my mother leads a completely active, normal life when so many others are struggling just to live on a day by day basis from their MS? Why is it that she can still live out her hopes and dreams to the fullest and chase after them on her own two feet unassisted, when so many others are on their way to bed rest? The answer? The answer is Prokarin™.
Prokarin™ is a medication which my mother developed when she was not willing to let her disease ruin her life. She found that if she used Prokarin™ on a daily basis her symptoms of MS reversed back to the quality of life she had prior to being diagnosed with MS in 1988.
So why if Prokarin™ gave my mother back her life, why are so many others still at the mercy of their MS? Big pharmaceutical companies are to blame. Prokarin™ is almost ten times cheaper than the MS drugs on the market today, has relatively no side effects in comparison to their drugs' long list of side effects, and does not just slow the progression of the disease, but in many testimonials, has reversed the debilitating symptoms of MS. Patients using Prokarin™ have reported stopping the pharmaceutical's money making drugs once on Prokarin™ as they no longer were in need of them, and for that reason, pharmaceuticals have shunned Prokarin™ and tried to hide it from the MS public. This is my reasoning behind writing this whole blog. I want to get the word out to as many people as possible about Prokarin™ as I truly feel that even if you yourself do not have MS, there is a great chance that a friend of a friend of yours does and could get their life back possibly with the information below...
Prokarin™ is a cream that's applied to a patch, or more recently, its a disk which is worn on the skin daily. It costs only about $200.00 a month and in most cases, insurance is now picking up the cost. Patients using Prokarin™, especially those who are sensitive to heat, have reported seeing results ranging from decreased numbness, tingling, weakness and fatigue all the way up to walking again unassisted.
Prokarin™ you should know, has not been approved yet by the FDA, and for that reason, I cannot make claims regarding its effects. All I can say is what has been reported to me from patients on the drug, such as the above results I stated and tell you what miraculous results I see in my own mother each and every day, when she at times can even out run myself.
MS has stripped so many individuals and families of their hopes, dreams and loved ones and it doesn't have to be that way. Instead of Multiple Sclerosis being a prolonged death sentence, it can be simply a small inconvenience of having to remember to put a disk on before running out the door to fulfill your life.....
If you want more information on Prokarin™ you can visit the website www.edmsllc.com or call 1-866-222-3367.